ClinVar Miner

List of variants in gene KCNQ2 reported as likely benign for not provided

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Gene type:
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Total variants: 75
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HGVS dbSNP
NC_000020.11:g.63442560_63442562del rs374464103
NM_172107.4(KCNQ2):c.-150C>A rs554261385
NM_172107.4(KCNQ2):c.1056G>A (p.Ser352=) rs769146180
NM_172107.4(KCNQ2):c.1119-6T>C rs1022260777
NM_172107.4(KCNQ2):c.1119-7T>C rs953495853
NM_172107.4(KCNQ2):c.1137C>T (p.Tyr379=) rs781144303
NM_172107.4(KCNQ2):c.1194G>A (p.Lys398=) rs763988707
NM_172107.4(KCNQ2):c.1209C>T (p.Leu403=) rs752280961
NM_172107.4(KCNQ2):c.1218-12dup rs761233540
NM_172107.4(KCNQ2):c.1224C>T (p.Asp408=) rs1060503977
NM_172107.4(KCNQ2):c.123G>C (p.Leu41=) rs1600886191
NM_172107.4(KCNQ2):c.1247+304C>T rs545236920
NM_172107.4(KCNQ2):c.1248-4C>T rs772465626
NM_172107.4(KCNQ2):c.1290C>T (p.Pro430=) rs951436020
NM_172107.4(KCNQ2):c.1301+7C>T rs374877247
NM_172107.4(KCNQ2):c.1301+8G>A rs532111320
NM_172107.4(KCNQ2):c.1308G>A (p.Lys436=) rs1008990254
NM_172107.4(KCNQ2):c.144C>T (p.Pro48=) rs1600886044
NM_172107.4(KCNQ2):c.1506G>A (p.Ala502=) rs780293757
NM_172107.4(KCNQ2):c.1512G>A (p.Arg504=) rs750635636
NM_172107.4(KCNQ2):c.1525+199A>G rs112733886
NM_172107.4(KCNQ2):c.1526-107C>T rs76685684
NM_172107.4(KCNQ2):c.1526-7C>G rs761567082
NM_172107.4(KCNQ2):c.1539C>T (p.Pro513=) rs376713245
NM_172107.4(KCNQ2):c.1593C>T (p.Asp531=) rs1601569482
NM_172107.4(KCNQ2):c.1605C>T (p.Gly535=) rs767958822
NM_172107.4(KCNQ2):c.1632-7C>T rs779543926
NM_172107.4(KCNQ2):c.1678C>A (p.Arg560=) rs773171451
NM_172107.4(KCNQ2):c.1689C>T (p.Asp563=) rs35450031
NM_172107.4(KCNQ2):c.1698C>T (p.Asp566=) rs768228902
NM_172107.4(KCNQ2):c.1764-294C>T rs142360631
NM_172107.4(KCNQ2):c.1827C>T (p.Ala609=) rs369438374
NM_172107.4(KCNQ2):c.1842C>T (p.Pro614=) rs552807375
NM_172107.4(KCNQ2):c.1866G>C (p.Arg622=) rs1060503976
NM_172107.4(KCNQ2):c.1869C>T (p.Leu623=) rs774516728
NM_172107.4(KCNQ2):c.1887+10G>T rs1422499897
NM_172107.4(KCNQ2):c.1929C>T (p.Ile643=)
NM_172107.4(KCNQ2):c.1959A>G (p.Thr653=) rs563758575
NM_172107.4(KCNQ2):c.2037T>C (p.His679=) rs1162099839
NM_172107.4(KCNQ2):c.2064G>A (p.Lys688=) rs1266457198
NM_172107.4(KCNQ2):c.2067C>T (p.Ile689=) rs766273173
NM_172107.4(KCNQ2):c.2087C>T (p.Thr696Met) rs570139975
NM_172107.4(KCNQ2):c.2109G>A (p.Ala703=) rs771679143
NM_172107.4(KCNQ2):c.2145C>G (p.Ser715=) rs1601543762
NM_172107.4(KCNQ2):c.2172G>A (p.Pro724=) rs368268958
NM_172107.4(KCNQ2):c.2181C>T (p.Gly727=) rs1025748805
NM_172107.4(KCNQ2):c.2244C>T (p.His748=) rs376327268
NM_172107.4(KCNQ2):c.2265C>T (p.Tyr755=) rs563437123
NM_172107.4(KCNQ2):c.2316G>A (p.Pro772=) rs587780367
NM_172107.4(KCNQ2):c.2328C>T (p.Pro776=) rs1601542678
NM_172107.4(KCNQ2):c.2358G>A (p.Thr786=) rs559610397
NM_172107.4(KCNQ2):c.2376C>T (p.Ser792=) rs765593192
NM_172107.4(KCNQ2):c.2505G>C (p.Ala835=) rs764615246
NM_172107.4(KCNQ2):c.2523C>T (p.Thr841=) rs760979156
NM_172107.4(KCNQ2):c.2577G>A (p.Glu859=) rs1601541438
NM_172107.4(KCNQ2):c.2583C>A (p.Pro861=) rs1601541414
NM_172107.4(KCNQ2):c.297-10C>G rs763193303
NM_172107.4(KCNQ2):c.303C>T (p.Leu101=) rs145415996
NM_172107.4(KCNQ2):c.309T>C (p.Val103=) rs1600796985
NM_172107.4(KCNQ2):c.315C>T (p.Ser105=) rs200224824
NM_172107.4(KCNQ2):c.387+10G>A rs371918220
NM_172107.4(KCNQ2):c.387+24G>T rs113724995
NM_172107.4(KCNQ2):c.388-51C>T rs112315649
NM_172107.4(KCNQ2):c.444A>G (p.Ala148=) rs1365973227
NM_172107.4(KCNQ2):c.477G>T (p.Gly159=) rs757792092
NM_172107.4(KCNQ2):c.515-4G>C rs1600786663
NM_172107.4(KCNQ2):c.552C>T (p.Ala184=) rs764119402
NM_172107.4(KCNQ2):c.691-5C>T rs886056921
NM_172107.4(KCNQ2):c.729C>T (p.Leu243=) rs755940771
NM_172107.4(KCNQ2):c.813C>T (p.Gly271=) rs1600766224
NM_172107.4(KCNQ2):c.817-5C>T rs774780027
NM_172107.4(KCNQ2):c.840C>T (p.Tyr280=) rs201556105
NM_172107.4(KCNQ2):c.867C>T (p.Asn289=) rs749934609
NM_172107.4(KCNQ2):c.915C>T (p.Phe305=) rs775918190
NM_172107.4(KCNQ2):c.918G>A (p.Ala306=) rs370777198

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